Canonical Allele Identifier: CA425415732

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597942T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375075T>C , CM000664.2:g.27375075T>C	GRCh38
NC_000002.11:g.27597942T>C , CM000664.1:g.27597942T>C	GRCh37
NC_000002.10:g.27451446T>C	NCBI36
NG_009305.1:g.383A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.696T>C MANE Select	ENSP00000233575.2:p.Ile232=
ENST00000233575.6:c.696T>C	ENSP00000233575.2:p.Ile232=
ENST00000427123.5:c.*506T>C	ENSP00000405399.1:n.*506T>C
ENST00000440760.5:c.*541T>C	ENSP00000399727.1:n.*541T>C
ENST00000453453.1:c.*223T>C	ENSP00000401922.1:n.*223T>C
ENST00000493711.1:n.413T>C
ENST00000494893.5:n.872T>C
ENST00000537606.5:c.621T>C	ENSP00000439208.1:p.Ile207=
NM_001267059.1:c.660T>C	NP_001253988.1:p.Ile220=
NM_001267060.1:c.621T>C	NP_001253989.1:p.Ile207=
NM_001267061.1:c.636T>C	NP_001253990.1:p.Ile212=
NM_014748.3:c.696T>C	NP_055563.1:p.Ile232=
NR_049782.1:n.1069T>C
NR_049783.1:n.1042T>C
NR_049784.1:n.1018T>C
NR_049785.1:n.951T>C
NR_049786.1:n.900T>C
NR_049787.1:n.751T>C
NR_049788.1:n.681T>C
XM_011533203.1:c.54T>C	XP_011531505.1:p.Ile18=
XM_011533203.2:c.54T>C	XP_011531505.1:p.Ile18=
XM_017005405.2:c.54T>C	XP_016860894.1:p.Ile18=
NM_014748.4:c.696T>C MANE Select	NP_055563.1:p.Ile232=
NM_001267059.2:c.660T>C	NP_001253988.1:p.Ile220=
NM_001267061.2:c.636T>C	NP_001253990.1:p.Ile212=
NR_049782.2:n.949T>C
NR_049783.2:n.922T>C
NR_049784.2:n.898T>C
NR_049785.2:n.831T>C
NR_049786.2:n.780T>C
NR_049787.2:n.631T>C
NR_049788.2:n.561T>C
NM_001267060.2:c.621T>C	NP_001253989.1:p.Ile207=